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Showing results (81-90 of 143) with videos related to

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Clinical and Laboratory Haematology|March 1, 1997
Diagnosis strategies in activated protein C resistance: is genotyping still necessary?C Biron, H Lamarti, J F Schved, et al.
Human Genetics|April 17, 1998
Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation testS Tuffery, S Chambert, C Bareil, et al.
Molecular Human Reproduction|February 6, 2003
First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markersA Girardet, S Hamamah, T Anahory, et al.
The Journal of Biological Chemistry|February 1, 2000
A naturally occurring sequence variation that creates a YY1 element is associated with increased cystic fibrosis transmembrane conductance regulator gene expressionM C Romey, N Pallares-Ruiz, A Mange, et al.
Gut|February 19, 2000
Is isolated idiopathic pancreatitis associated with CFTR mutations?N Pallares-Ruiz, S Carles, M des Georges, et al.
American Journal of Human Genetics|January 13, 2000
Meiotic segregation analysis of RB1 alleles in retinoblastoma pedigrees by use of single-sperm typingA Girardet, M S McPeek, E P Leeflang, et al.
The New England Journal of Medicine|February 11, 1993
High frequency of the R117H cystic fibrosis mutation in patients with congenital absence of the vas deferensR Gervais, V Dumur, J M Rigot, et al.
Annals of Neurology|August 17, 2001
Nonprogressive autosomal recessive ataxia maps to chromosome 9q34-9qter in a large consanguineous Lebanese familyV Delague, C Bareil, P Bouvagnet, et al.
Clinical and Laboratory Haematology|March 1, 1994
Direct carrier testing of haemophilia B by SSCPP A Martinez, M C Romey, J F Schved, et al.
Molecular Human Reproduction|June 13, 2003
Specific detection of deleted and non-deleted dystrophin exons together with gender assignment in preimplantation genetic diagnosis of Duchenne muscular dystrophyA Girardet, S Hamamah, H Déchaud, et al.
Pageof 15

Showing results (81-90 of 143) with videos related to

Sort By:
Pageof 15
Clinical and Laboratory Haematology|March 1, 1997
Diagnosis strategies in activated protein C resistance: is genotyping still necessary?C Biron, H Lamarti, J F Schved, et al.
Human Genetics|April 17, 1998
Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation testS Tuffery, S Chambert, C Bareil, et al.
Molecular Human Reproduction|February 6, 2003
First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markersA Girardet, S Hamamah, T Anahory, et al.
The Journal of Biological Chemistry|February 1, 2000
A naturally occurring sequence variation that creates a YY1 element is associated with increased cystic fibrosis transmembrane conductance regulator gene expressionM C Romey, N Pallares-Ruiz, A Mange, et al.
Gut|February 19, 2000
Is isolated idiopathic pancreatitis associated with CFTR mutations?N Pallares-Ruiz, S Carles, M des Georges, et al.
American Journal of Human Genetics|January 13, 2000
Meiotic segregation analysis of RB1 alleles in retinoblastoma pedigrees by use of single-sperm typingA Girardet, M S McPeek, E P Leeflang, et al.
The New England Journal of Medicine|February 11, 1993
High frequency of the R117H cystic fibrosis mutation in patients with congenital absence of the vas deferensR Gervais, V Dumur, J M Rigot, et al.
Annals of Neurology|August 17, 2001
Nonprogressive autosomal recessive ataxia maps to chromosome 9q34-9qter in a large consanguineous Lebanese familyV Delague, C Bareil, P Bouvagnet, et al.
Clinical and Laboratory Haematology|March 1, 1994
Direct carrier testing of haemophilia B by SSCPP A Martinez, M C Romey, J F Schved, et al.
Molecular Human Reproduction|June 13, 2003
Specific detection of deleted and non-deleted dystrophin exons together with gender assignment in preimplantation genetic diagnosis of Duchenne muscular dystrophyA Girardet, S Hamamah, H Déchaud, et al.
Pageof 15